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FDA 510(k)

Solax Electric Scooter (Models: S204311M, S204161, S204143)

K-Number: K190737 · 2021-05-10

ApplicantDongguan Prestige Sporting Goods Co., Ltd.
Decision Date2021-05-10
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Solax Electric Scooter (Models: S204311M, S204161, S204143) is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-05-10 under approval number K190737. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Solax Electric Scooter (Models: S204311M, S204161, S204143)?

Solax Electric Scooter (Models: S204311M, S204161, S204143) is a medical device that received FDA 510(k) clearance on 2021-05-10. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K190737.

When was Solax Electric Scooter (Models: S204311M, S204161, S204143) approved by the FDA?

Solax Electric Scooter (Models: S204311M, S204161, S204143) received FDA 510(k) clearance on 2021-05-10, under approval number K190737.

What company makes Solax Electric Scooter (Models: S204311M, S204161, S204143)?

Solax Electric Scooter (Models: S204311M, S204161, S204143) is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..

What is the FDA product code for Solax Electric Scooter (Models: S204311M, S204161, S204143)?

The FDA product code for Solax Electric Scooter (Models: S204311M, S204161, S204143) is INI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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